Macromolecules, volume 34, issue 22, pages 7624-7628

Asymmetric Polymerization of Dialdehyde and Bis(allylsilane) in the Presence of Chiral (Acyloxy)borane Catalyst

Publication typeJournal Article
Publication date2001-09-28
Journal: Macromolecules
scimago Q1
SJR1.401
CiteScore9.3
Impact factor5.1
ISSN00249297, 15205835
Materials Chemistry
Organic Chemistry
Inorganic Chemistry
Polymers and Plastics
Abstract
We present a study of the asymmetric polymerization of dialdehyde and bis(allylsilane) based on the enantioselective addition of allylsilane to aldehyde in the presence of chiral Lewis acid. Chiral (acyloxy)borane (CAB) derived from enantiopure tartaric acid was used as a chiral Lewis acid to promote the asymmetric polymerization. Repetitive allylation reaction between these monomers in the presence of CAB yielded optically active polymers having asymmetric carbons in their main chain. The corresponding model asymmetric reaction of β-substituted allylsilane with benzaldehyde was also studied.
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